Last synced on 10 January 2025 at 11:05 pm

Reverso

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212107
510(k) Type
Traditional
Applicant
Intelis Instruments Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
11/10/2021
Days to Decision
127 days
Submission Type
Summary

Reverso

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212107
510(k) Type
Traditional
Applicant
Intelis Instruments Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
11/10/2021
Days to Decision
127 days
Submission Type
Summary